1. CMU Intellectual Repository

Browsing by Author Piranit N. Kantaputra

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 14 of 14
Issue DateTitleAuthor(s)
1-Apr-2019ADAMTSL1 and mandibular prognathismPiranit N. Kantaputra; Apitchaya Pruksametanan; Nattapol Phondee; Athiwat Hutsadaloi; Worrachet Intachai; Katsushig Kawasaki; Atsushi Ohazama; Chumpol Ngamphiw; Sissades Tongsima; James R. Ketudat Cairns; Polbhat Tripuwabhrut
1-Dec-2006Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletionPiranit N. Kantaputra; Chanin Limwongse; Chintana Tochareontanaphol; Apiwat Mutirangura; Umnat Mevatee; Verayuth Praphanphoj
1-Jul-2010Corrigendum to obesity syndrome, MOMES caused by deletion-duplication (4q35.1 del and 5p14.3 duplication) (American Journal of Medical Genetics Part A (2009) 149, 4, (833-834))Mieke M. Van Haelst; Rubin Wang; Piranit N. Kantaputra; Rodger Palmer; Philip Beales
1-Jan-2018Genetic regulatory pathways of split-hand/foot malformationPiranit N. Kantaputra; Bruce M. Carlson
1-Dec-2010Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2qPiranit N. Kantaputra; Eva Klopocki; Bianca P. Hennig; Verayuth Praphanphoj; Cédric Le Caignec; Bertrand Isidor; Mei L. Kwee; Deborah J. Shears; Stefan Mundlos
20-Sep-2019Missense Pathogenic variants in KIF4A Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-InvaginatusLord J.J. Gowans; Sophia Cameron-Christie; Rebecca L. Slayton; Tamara Busch; Miguel Romero-Bustillos; Steven Eliason; Mason Sweat; Nara Sobreira; Wenjie Yu; Piranit N. Kantaputra; Elizabeth Wohler; Wasiu Lanre Adeyemo; Salil A. Lachke; Deepti Anand; Collen Campbell; Bernadette K. Drummond; David M. Markie; W. Jansen van Vuuren; L. Jansen van Vuuren; Paul S. Casamassimo; Ronald Ettinger; Arwa Owais; I. van Staden; Brad A. Amendt; Adebowale A. Adeyemo; Jeffrey C. Murray; Stephen P. Robertson; Azeez Butali
1-Jun-2011Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palatePiranit N. Kantaputra; Sutti Malaivijitnond; Alexandre R. Vieira; Jan Heering; Volker Dötsch; Theerapong Khankasikum; Warissara Sripathomsawat
1-Dec-2006A newly recognized polyosteolysis/hyperostosis syndromePiranit N. Kantaputra; Chanin Limwongse; Ajchara Koolvisoot; Apichart Ausawamongkolkul; Somsiri Tayavitit
1-Jan-2005A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?Piranit N. Kantaputra; Pranoot Tanpaiboon
1-Nov-2010A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromePiranit N. Kantaputra; Stefan Mundlos; Warissara Sripathomsawat
1-Apr-2009Obesity Syndrome, MOMES caused by deletion-duplication (4q35.1 del and 5p14.3 dup)Mieke M. Van Haelst; Rubin Wang; Piranit N. Kantaputra; Rodger Palmer; Philip Beales
1-Mar-2019Oral manifestations in patients and dogs with mucopolysaccharidosis Type VIIPiranit N. Kantaputra; Lachlan J. Smith; Margret L. Casal; Chulaluck Kuptanon; Yu Cheng Chang; Sheela Nampoothiri; Apichai Paiyarom; Thanat Veerasakulwong; Objoon Trachoo; James R. Ketudat Cairns; Wannapa Chinadet; Pranoot Tanpaiboon
1-Jan-2012Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutationPiranit N. Kantaputra; Oranart Matangkasombut; Warissara Sripathomsawat
1-Sep-2009ΔNp63 knockdown mice: A mouse model for AEC syndromeMaranke I. Koster; Barbara Marinari; Aimee S. Payne; Piranit N. Kantaputra; Antonio Costanzo; Dennis R. Roop
Showing results 1 to 14 of 14